氢溢流
催化作用
氢
选择性
拉曼光谱
溢出效应
材料科学
原位
化学工程
纳米技术
化学
光化学
制作
无机化学
有机化学
工程类
微观经济学
病理
光学
经济
物理
医学
替代医学
作者
Jie Wei,Si‐Na Qin,Jingli Liu,Xiangyu Ruan,Zhiqiang Guan,Hao Yan,Diye Wei,Hua Zhang,Jun Cheng,Hongxing Xu,Zhong‐Qun Tian,Jian‐Feng Li
标识
DOI:10.1002/anie.202000426
摘要
The spillover of hydrogen species and its role in tuning the activity and selectivity in catalytic hydrogenation have been investigated in situ using surface-enhanced Raman spectroscopy (SERS) with 10 nm spatial resolution through the precise fabrication of Au/TiO2 /Pt sandwich nanostructures. In situ SERS study reveals that hydrogen species can efficiently spillover at Pt-TiO2 -Au interfaces, and the ultimate spillover distance on TiO2 is about 50 nm. Combining kinetic isotope experiments and density functional theory calculations, it is found that the hydrogen spillover proceeds via the water-assisted cleavage and formation of surface hydrogen-oxygen bond. More importantly, the selectivity in the hydrogenation of the nitro or isocyanide group is manipulated by controlling the hydrogen spillover. This work provides molecular insights to deepen the understanding of hydrogen activation and boosts the design of active and selective catalysts for hydrogenation.
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